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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1395843Generated: October 25, 2026

3,4-Dichloro-2-hydroxybenzoic acid → Phenylalanine ethyl ester

https://huagongshe.com/reaction/1395843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Dichloro-2-hydroxybenzoic acidHCID 29078103—
ReactantN-(2-hydroxy-3,5-dichlorobenzoyl)-L-phenylalanineHCID 51037939—
Reactant2-Acetoxyacetoxy-3,5-dichlorobenzoic acidHCID 66906292—
Reactant2-Acetoxyacetoxy-3,5-dichlorobenzoic acid chlorideHCID 87198957—
ProductPhenylalanine ethyl esterHCID 76506—
ProductN-(2-acetoxy-3,5-dichlorobenzoyl)-L-phenylalanineHCID 66906696—
Product2-Acetoxyacetoxy-3,5-dichlorobenzoic acid chlorideHCID 87198957—

Reaction Steps

The invention also provides a method for synthesizing N-(2-hydroxy-3,5-dichlorobenzoyl)-L-phenylalanine, comprising: converting 3-5 dichlorosalicylic acid into 2-acetoxy-acetoxy-3,5-dichlorobenzoic acid; converting 2-acetoxyacetoxy-3,5-dichlorobenzoic acid into 2-acetoxyacetoxy-3,5-dichlorobenzoic acid chloride; reacting 2-acetoxyacetoxy-3,5-dichlorobenzoic acid chloride with L-phenylalanine ethyl ester to form N-(2-acetoxy-3,5-dichlorobenzoyl)-L-phenylalanine; and converting N-(2-acetoxy-3,5-dichlorobenzoyl)-L-phenylalanine into N-(2-hydroxy-3,5-dichlorobenzoyl)-L-phenylalanine. In some embodiments, the converting comprises hydrolyzing of ester functions in N-(2-acetoxy-3,5-dichlorobenzoyl)-L-phenylalanine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045274E1
Source datasetuspto-grants-2014_12
ORD IDord-da1b323c44934551b0432b43961664ac
Source noteuspto-grants-2014_12